Company ยท US
Avantis Medical Systems, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2016. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| FDF | Colonoscope And Accessories, Flexible/Rigid | 6 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 17, 2016 | K160356 | Third Eye Panoramic Auxiliary Endoscopy System - Resposable Avantis Medical Systems, Inc. | FDF |
| Nov 17, 2014 | K140595 | THIRD EYE PANORAMIC AUXILIARY ENDOSCOPY SYSTEM Avantis Medical Systems, Inc. | FDF |
| Nov 5, 2009 | K093187 | MODIFICATION TO THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM Avantis Medical Systems, Inc. | FDF |
| Jul 7, 2009 | K091783 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPE SYSTEM Avantis Medical Systems, Inc. | FDF |
| Feb 12, 2009 | K083180 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM Avantis Medical Systems, Inc. | FDF |
| Apr 24, 2007 | K070330 | THIRD EYE RETROSCOPE AUXILIARY ENDOSCOPY SYSTEM Avantis Medical Systems, Inc. | FDF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||